Muscular Dystrophy - OG
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Transcript Muscular Dystrophy - OG
By: Isabelle Masloski
and
Will Michels
Period 4
Muscular
Dystrophy is an inherited
disorder where your muscles weaken
and tissue is loss.
It continually gets worse over time.
Guillaume
Benjamin Amand Duchenne
discovered Muscular Dystrophy.
It was discovered in the 1860’s in Paris.
He described 7 progressive muscle
weakness in 13 young boys.
It was later called Duchenne Muscular
Dystrophy after Benjamin.
Difficulty
using one
or more muscle
groups
Muscle weakness that
slowly gets worse
Frequent Falling
Loss in muscle size
No
cure
Treatment is used to
prevent symptoms.
Physical therapy can
help keep muscle
strength
Braces improve
mobility
Staying active is key,
bed rest could make
the disease worse
Doctors
use your past medical records and
physical examines to determine if someone
has muscular dystrophy and what type.
Some types are:
• Becker muscular dystrophy
• Duchenne muscular dystrophy(most common in
children)
• Emery-Dreifuss muscular dystrophy
• Limb-girdle muscular dystrophy
• Myotonic dystrophy(most common in adults)
A
Muscle Biopsy or DNA blood tests can
affirm the diagnosis.
It is passed down
through families by an
affected gene.
Different types are
passed down different
ways.
Limb-girdle dystrophy
is autosomal recessive
Duchenne dystrophy is
a defective gene
carried by the female
and transmitted to the
male.
Each type affects a
different gene.
1
in 3 thousand
children are born
with Duchenne
muscular disease.
Average lifespan for
those with Duchenne
MD is about 20 years,
but those with Becker
MD can have a
normal lifespan.
Van Wyk , Andre. "10 Muscular Dystrophy Facts."
Health24. N.p., 26 June 2012. Web. 23 February 2013.
Kaneshiro, Neil. Ed. "Muscular Dystrophy." The New York
Times. N.p., 21 February 2012. Web. 23 February 2013.
Neurol, Can J. "Duchenne De Boulogne: a pioneer in
neurology and medical photography." NCBI. N.p., August
2005. Web. 23 February 2013